Vega Yaiza Hernández, Smith Anna, Cockerill Hannah, Tang Shan, Agirre-Arrizubieta Zaloa, Goyal Sushma, Pina Marisa, Akman Cigdem I, Jolleff Nicola, McGinnity Colm, Gomez Kumudini, Gupta Rajesh, Hughes Elaine, Jackman John, McCormick David, Oren Caroline, Scott David, Taylor Jacqueline, Trounce John, Clarke Tara, Kugler Steven, Mandelbaum David E, McGoldrick Patricia, Wolf Steven, Strug Lisa J, Pal Deb K
King's College London, UK.
King's College London, UK; King's Health Partners, London, UK.
Epilepsy Behav. 2015 Dec;53:174-9. doi: 10.1016/j.yebeh.2015.10.016. Epub 2015 Nov 12.
The high prevalence and impact of neurodevelopmental comorbidities in childhood epilepsy are now well known, as are the increased risks and familial aggregation of reading disability (RD) and speech sound disorder (SSD) in rolandic epilepsy (RE). The risk factors for RD in the general population include male sex, SSD, and ADHD, but it is not known if these are the same in RE or whether there is a contributory role of seizure and treatment-related variables.
An observational study of 108 probands with RE (age range: 3.6-22 years) and their 159 siblings (age range: 1-29 years; 83 with EEG data) were singly ascertained in the US or UK through a proband affected by RE. We used a nested case-control design, multiple logistic regression, and generalized estimating equations to test the hypothesis of an association between RD and seizure variables or antiepileptic drug treatment in RE; we also assessed an association between EEG focal sharp waves and RD in siblings.
Reading disability was reported in 42% of probands and 22% of siblings. Among probands, RD was strongly associated with a history of SSD (OR: 9.64, 95% CI: 2.45-37.21), ADHD symptoms (OR: 10.31, 95% CI: 2.15-49.44), and male sex (OR: 3.62, 95% CI: 1.11-11.75) but not with seizure or treatment variables. Among siblings, RD was independently associated only with SSD (OR: 4.30, 95% CI: 1.42-13.0) and not with the presence of interictal EEG focal sharp waves.
The principal risk factors for RD in RE are SSD, ADHD, and male sex, the same risk factors as for RD without epilepsy. Seizure or treatment variables do not appear to be important risk factors for RD in probands with RE, and there was no evidence to support interictal EEG focal sharp waves as a risk factor for RD in siblings. Future studies should focus on the precise neuropsychological characterization of RD in families with RE and on the effectiveness of standard oral-language and reading interventions.
儿童癫痫中神经发育共病的高患病率及其影响现已为人熟知,罗兰多癫痫(RE)中阅读障碍(RD)和语音障碍(SSD)的风险增加及家族聚集性情况也同样如此。普通人群中RD的风险因素包括男性、SSD和注意力缺陷多动障碍(ADHD),但尚不清楚在RE中这些因素是否相同,或者癫痫发作及治疗相关变量是否起作用。
通过一名患RE的先证者在美国或英国单独确定了108名RE先证者(年龄范围:3.6 - 22岁)及其159名兄弟姐妹(年龄范围:1 - 29岁;83名有脑电图数据)。我们采用巢式病例对照设计、多重逻辑回归和广义估计方程来检验RE中RD与癫痫发作变量或抗癫痫药物治疗之间存在关联的假设;我们还评估了兄弟姐妹中脑电图局灶性尖波与RD之间的关联。
42%的先证者和22%的兄弟姐妹报告有阅读障碍。在先证者中,RD与SSD病史(比值比:9.64,95%置信区间:2.45 - 37.21)、ADHD症状(比值比:10.31,95%置信区间:2.15 - 49.44)和男性(比值比:3.62,95%置信区间:1.11 - 11.75)密切相关,但与癫痫发作或治疗变量无关。在兄弟姐妹中,RD仅独立与SSD相关(比值比:4.30,95%置信区间:1.42 - 13.0),与发作间期脑电图局灶性尖波的存在无关。
RE中RD的主要风险因素是SSD、ADHD和男性,与无癫痫的RD风险因素相同。癫痫发作或治疗变量似乎不是RE先证者中RD的重要风险因素,且没有证据支持发作间期脑电图局灶性尖波是兄弟姐妹中RD的风险因素。未来的研究应聚焦于RE家庭中RD的精确神经心理学特征以及标准口语和阅读干预的有效性。